Method for NMR spectroscopy with sustained induction decays of long-lived coherences

ABSTRACT

A method for nuclear magnetic resonance (NMR) spectroscopy of a sample involves excitation of long lived coherences (LLC) between the singlet state S 0  and the central triplet state T 0  of nuclei of the sample by initiating irradiation of the sample with an rf-field with carrier frequency ω rf ; sustaining of the LLC by maintaining the rf-irradiation during an interval τ 2 ; converting the LLC temporarily into observable magnetisation by interrupting the rf-irradiation during an observation interval τ 3 ; detecting NMR-signals during the observation interval τ 3  and reconversion of the observable magnetisation back into LLC after the observation interval τ 3 . These steps are repeated n times, wherein n is a positive integer. The method allows ultra high-resolution spectra of long-lived coherences to be obtained.

This application claims Paris convention priority of EP 11 165 564.3 filed May 10, 2011, the entire disclosure of which is hereby incorporated by reference.

BACKGROUND OF THE INVENTION

The invention concerns a method for nuclear magnetic resonance (NMR) spectroscopy of a sample comprising the following steps:

-   (a) excitation of long lived coherences (LLC) between the singlet     state S₀ and the central triplet state T₀ of nuclei of the sample by     initiating irradiation of the sample with an rf-field with a carrier     frequency; -   (b) sustaining of the LLC by maintaining the rf-irradiation during     an interval τ₂; -   (c) converting the LLC temporarily into observable magnetisation by     interrupting the rf-irradiation during an observation interval τ₃; -   (d) detecting NMR-signals during the observation interval τ₃.

Most nuclear magnetic resonance (NMR) methods employ Fourier transformations of free induction decays (FID's).¹ Though widely used, this approach suffers from homogeneous decay and imperfect homogeneity of a static magnetic field, so that it is challenging to achieve line-widths below 1 Hz.² Sophisticated NMR pulse sequences have been developed to achieve reasonable line-widths (1<Δν<50 Hz) in moderately inhomogeneous fields, exploiting cross relaxation effects³, observation in the earth's magnetic field⁴, or a spatial correlation between the static and radio-frequency (rf) field profiles⁵. By combining refocusing and coherence transfer through couplings, one can obtain acceptable line-widths (1<Δν<50 Hz) even in very inhomogeneous fields (Δν>2 kHz).⁶ In systems with two scalar-coupled homonuclear spins I=½ and S=½, one can excite long-lived coherences (LLC's) that can have very long life-times T_(LLC) and hence very narrow line-widths Δν_(LLC)=1/(π/T_(LLC)).⁷⁻⁹ Their precession frequency is independent of offset (and hence of chemical shifts and inhomogeneous broadening) and is only determined by the sum of scalar and residual dipolar couplings (T_(IS)=J_(IS)+2D_(IS)). So far, LLC's have only been observed indirectly in the manner of two-dimensional (2D) spectroscopy, i.e. point by point, either in combination with field cycling⁷ or in high field.⁸⁻⁹

Principles

Long-lived coherences (LLC's) constitute a class of zero-quantum coherences that can be excited by extremely low frequency fields (ELF's) in a vanishing static field.⁷ LLC's can also be excited in high fields by creating a state where the coherences I_(y) and −S_(y) have opposite phases, so that they can be locked by a continuous ‘sustaining’ rf field⁸⁻⁹. This rf field in effect suppresses the chemical shifts, thus rendering the spins magnetically equivalent, so that their eigenstates can be classified according to ‘symmetrical’ and ‘antisymmetrical’ irreducible representations of the spin permutation group. LLC's span zero-quantum transitions between states of different symmetry. Their oscillatory decays can be subjected to a Fourier transformation, yielding doublets that are reminiscent of ‘J-spectroscopy’¹¹⁻¹³. The life-times T_(LLC) of LLC's can be a factor κ longer than the transverse relaxation times T₂=T_(SQC) of ordinary single-quantum coherences (T_(LLC)=κT₂), so that the line-widths Δν_(LLC)=1/(πT_(LLC)) can be narrower by a factor Δν_(LLC)/Δν_(SQC)=1/κ. Depending on the role of extraneous relaxation mechanisms⁹, one can expect κ≦3 in small molecules in the extreme narrowing limit, and κ≦9 in the slow¹⁴ motion limit typical of large molecules. In practice, we have observed 2.5<κ<4.3 over a range of correlation times.¹⁵

Generally speaking, LLC's should not be confused with long-lived states (LLS's), also known as singlet states (SS) if there are only two spins in the system. LLS's refer to populations of antisymmetric singlet states¹⁶⁻²⁸. LLS's have life-times that can be much longer than LLC's (T_(LLS)>>T_(LLC)), but do not have any oscillatory character, and cannot give rise to J-spectra in the manner of LLC's. Both LLS's and LLC's can be temporarily converted into observable magnetisation (vide infra). This is of particular interest when the initial polarization is enhanced by ‘dissolution’ DNP^(10,21).

If the oscillatory decays of LLC's are observed point-by-point in the manner of two-dimensional (2D) spectroscopy, they cannot be enhanced (‘hyperpolarized’) by ‘dissolution’ DNP. Recently, several 2D experiments have been successfully converted into ‘ultra-fast’ versions that can be combined with ‘dissolution’ DNP.²²⁻²³ However, the continuous rf field, which is preferably used to sustain LLC's is not compatible with current ‘ultra-fast’ schemes.

It is an object of the present invention to propose a method that allows obtaining ultra high-resolution spectra of long-lived coherences with enhanced resolution.

SUMMARY OF THE INVENTION

This object is achieved by:

(e) reconverting the observable magnetisation back into LLC after the observation interval τ₃; and repeating steps (b)-(e) n times, with n is a positive integer.

The irradiation of step (b) is resumed and the loop is repeated n times, where the integer n can be preferably 100 or more. It is clear for one who is skilled in the art that in the final repetition step (e) can be omitted without leaving the scope of the invention.

A long lived coherence (LLC) is a coherent superposition between the singlet and the central triplet state of two nuclei of the same kind. Long-lived coherences (LLC's) constitute a class of zero-quantum coherences. The excitation of LLC is carried out in a magnetic field, in particular in the magnetic field of the NMR magnet. Pairs of nuclei are chosen from the sample. The excitation of LLC comprises a transformation of an initial spin distribution (I_(z)+S_(z)) into (I_(x)−S_(x)) or (I_(y)−S_(y)) or (2I_(y)S_(z)−2I_(z)S_(y)) or (2I_(x)S_(z)-2I_(z)S_(x)) respectively just before the rf-field is applied, i.e. the initial spin distribution (I_(z)+_(Z)) is flipped to the transverse plane (observable magnetisation). The excitation can be achieved by various preparations, e.g., by applying a non-selective (π/2)_(x) or (π/2)_(y)-pulse or by applying a semi-selective π-pulse that affects only the multiplet of either spin I or spin S, followed by a non-selective (π/2)_(x) or (π/2)_(y)-pulse, or by using an echo sequence with a band-selective refocusing pulse, or by using a long lived state filter. Other preparations are also possible. (I_(x)−S_(x)) or (I_(y)−S_(y)) or (2I_(y)S_(z)−2I_(z)S_(y)) or (2I_(x)S_(z)-2I_(z)S_(x)) is then transformed into LLC by initiating irradiation of the rf-field. The LLC are sustained as long as rf-irradiation is applied.

When the rf-irradiation is interrupted, the LLC is no longer sustained, but converted into observable magnetisation, whereby “observable magnetisation” means magnetisation which is detectable by MR measurements (transverse magnetisation, in particular single quantum coherences (I_(x)−S_(x))). When the sustaining rf field is switched on again, the remaining observable magnetization (differences (I_(x)−S_(x)) or (I_(y)−S_(y)) or (2I_(y)S_(z)−2I_(z)S_(y)) or (2I_(x)S_(z)-2I_(z)S_(x))) are reconverted into LLC's, while the sum (I_(x)+S_(x)) or (I_(x)+S_(y)) is spin-locked and decays, and the sum 2I_(y)S_(z)+2I_(z)S_(y) is dephased under the effect of the rf field inhomogeneity. The repetition of sustaining of the rf-field, interrupting the rf-field and detecting NMR-signals during the observation interval results in partial decay of the LLC.

The RF irradiation can consist of a composite pulse scheme comprising a manifold of pulses and phases. Nevertheless the rf-irradiation is preferably carried out along an x-axis, if the LLC contains (I_(x)−S_(x)) terms and along the y-axis if the LLC contains (I_(y)−S_(y)) terms, whereby the x-axis and the y-axis of the rotating reference frame are both perpendicular to the z-direction of the static field, in which the experiment is carried out.

During the irradiation intervals τ₂, the coherence LLC evolves under the effect of the total coupling 2T_(IS)=2J_(IS)+4D_(IS) and decays with the relaxation rate R_(LLC)=1/T_(LLC). During each observation interval (observation window τ₃), the system evolves under the chemical shifts and again under the total coupling constant T_(IS), albeit reduced by a factor 2, and decays with the single-quantum relaxation rate R₂=1/T₂.

The duration τ3 of the observation interval can be equal for each repetition. Yet, it is also possible to choose non-constant durations for the observation interval (i.e. τ3 may be different in different repetitions) to achieve sparse sampling.

This invention shows that a signal comprising a larger number n of data points can be obtained in a single scan. With the inventive method, long-lived coherences (LLC's) in homonuclear pairs of chemically inequivalent spins can be excited and sustained during protracted radio-frequency irradiation periods that alternate with brief windows for signal observation (observation interval). Fourier transformation of the sustained induction decays recorded in a single scan yields NMR spectra with line-widths in the range 10<Δν<100 mHz, even in moderately inhomogeneous magnetic fields. If the windows for signal observation have a duration that is negligible compared to the protracted irradiation periods, the line-widths Δν approach the limiting line-widths Δν_(LLC). Even in poorly shimmed magnets where the inhomogeneous line width is Δν*>20 (protons) Hz, the inventive method can provide line-widths as narrow as Δν_(LLC)=14 mHz. The resulting doublets, which are reminiscent of 1-spectra, allow one to determine the sum of scalar and residual dipolar interactions in partly oriented media.

In a variant of the inventive method, the LLC are excited by transforming an initial spin polarization, (I_(z)+S_(z)), in particular the thermal equilibrium Boltzmann distribution, of the spin polarization (I_(z)+S_(z)) into single quantum coherences (I_(x)-S_(x)) or (I_(y)−S_(y)) or (2I_(y)S_(z)−2I_(z)S_(y)) or (2I_(z)S_(z)−2I_(z)S_(z)) prior to initiating irradiation of the sample with the rf-field.

Alternatively the sample is hyperpolarized, in particular by using dynamic nuclear polarization, thereby enhancing the spin polarization (I_(z)+S_(Z)) and the LLC that are subsequently excited by transforming the enhanced spin polarization (I_(z)+S_(z)) into enhanced single quantum coherences (I_(x)−S_(x)) or (I_(y)−S_(y)) or (2I_(y)S_(z)−2I_(z)S_(y)) or (2I_(z)S_(x)−2I_(z)S_(x)), prior to initiating irradiation of the sample with the rf-field. Thereby the signal to noise ratio can be improved.

In a preferred variant the carrier frequency is ω_(rf)=(Ω_(I)−Ω_(S))/2, with Ω_(I) chemical shift of nuclei of the sample with spin I, and Ω_(S) chemical shift of nuclei of the sample with spin S.

If the carrier frequency is chosen half-way between the two chemical shifts σ=−I_(y)−S_(y) is entirely transformed into σ=I_(x)−S_(x) during the preparation.

The rf-field is a preferably a continuous wave-rf-field. A continuous wave rf-field constitutes the simplest way to sustain the LLC.

In a special variant the rf-field is modulated in amplitude.

Alternatively or additionally the rf-field is modulated in phase.

It is preferred that that the amplitude of the rf-field is larger than the offset in, |Ω_(I)−Ω_(S)|/2.

In a highly preferred variant a refocusing pulse is applied in the middle of the observation interval τ₃. Contributions to the LLC from (I_(x)+S_(x)), (I_(y)+S_(y)) and (2I_(x)S_(z)+2I_(z)S_(x)) and (2I_(y)S_(z)+2I_(z)S_(y)), can be suppressed by using a π pulse in the middle of each window to refocus the chemical shifts. This enables a more accurate measurement of the scalar coupling J_(IS) and the total coupling T_(IS)=J_(IS)+2D_(IS) even for long observation intervals τ3, in particular 100 μs<τ₃<2 ms. Long observation intervals allow one to average over a larger number of data points in each window, resulting in improved signal-to-noise ratios. The detection of NMR-signals is preferably carried out during the first half τ₃/2 of the observation interval τ3. But it is also possible to detected NMR-signals in the second half τ₃/2 of the observation interval.

In a preferred variant the NMR spectroscopy measurement is carried out in a single experiment. A “single experiment” comprises one single preparation, i.e. only one single excitation of long lived coherences by applying rf-pulses.

Further advantages can be extracted from the description and the enclosed drawings. The features mentioned above and below can be used in accordance with the invention either individually or collectively in any combination. The embodiments mentioned are not to be understood as exhaustive enumeration but rather have exemplary character for the description of the invention.

BRIEF DESCRIPTION OF THE DRAWING

FIG. 1 shows pulse sequences for exciting and sustaining LLC's according to the invention. A complete pulse sequence comprises a preparation sequence and a sustaining/detection sequence. Each one of the four suggested preparation sequences A1-A4 allows one to create a density operator σ=I_(x)−S_(x). Either of the two sustaining/detection sequences B1 and B2 can be used to sustain the LLC's by CW irradiation and to acquire signals in the windows τ₃ or τ₃/2. The sustaining-acquisition blocks are repeated n times;

FIG. 2 shows examples of FID's and SID's recorded ‘on the fly’ by using the inventive method, together with their Fourier transforms:

-   -   a, Real part of a conventional ‘free induction decay’ (FID) due         to single-quantum coherences (SQC's) of the two protons of         2,3-dibromothiophene in a 20 mM isotropic solution in DMSO-d₆         with 30 mM ascorbic acid, measured at 11.7 T (500 MHz for         protons) and 296 K;     -   b, Conventional Fourier transform of the FID in (a), showing a         doublet with average line widths <Δν>≈1.5 Hz and a splitting         J_(IS)≈5.8 Hz;     -   c, Real part of the echo amplitude of 2,3-dibromothiophene in a         20 mM isotropic solution in DMSO-d₆ with 30 mM ascorbic acid         (note that the time scale was expanded by a factor 18 with         respect to (a)) which was measured with conventional J-resolved         ¹H spectroscopy²⁹;     -   d, Positive projection of the 2-dimensional Fourier transform,         showing a doublet with line widths <Δν>≈70 mHz and a splitting         J_(IS)≈5.77 Hz;     -   e, Real part of the ‘sustained induction decay’ (SID) of the two         protons of 2,3-dibromothiophene in a 20 mM isotropic solution in         DMSO-d₆ with 30 mM ascorbic acid acquired ‘on the fly’ in a         single scan according to the present invention (note that the         time scale was expanded by a factor 100 with respect to (a)),         arising from an LLC excited in the same sample with sequence A3         of FIG. 1, sustained and observed with sequence B2, The         parameters were τ₃/2=100 μs, Δt=τ₂+τ₃=50 ms, rf amplitude of the         CW sustaining field γB₁/(2π)=4.5 kHz, offsets         Ω1/(2π)=−Ω_(S)/(2π)=145 Hz, the rf carrier being set half-way         between the two chemical shifts;     -   f, Spectrum obtained by a real Fourier transformation of the SID         of (e), showing a doublet with line widths <Δν>≈16.4 mHz and a         splitting 2J_(IS)≈11.5286 Hz. If undesirable spin-locked         I_(x)+S_(X) terms had not been suppressed, they would give rise         to peak at v=0. The narrowest line-widths <Δν>=14 mHz (not         shown) were observed with scheme B1, τ₃=30 μs and Δt=τ₂+τ₃=50         ms;     -   g, Zoom of (d), with apparent scalar coupling constant J_(IS)         ^(app)=5764.3±0.2 mHz and <Δν>=16.4±0.1 mHz;     -   h, Zoom similar to (g) of an ‘on the fly’ LLC spectrum of the         two diastereotopic protons of glycine in L-Ala-Gly, with J_(IS)         ^(app)=17236.5±0.2 mHz and <Δν>=115.0±0.7 mHz;

FIG. 3 shows average life-times, apparent scalar couplings, and signal-to-noise ratios.

-   -   a, Average life-times <T>=1/<R> (see Eq. (4)) in the same sample         of 2,3-dibromothiophene as in FIG. 2, measured as a function of         the duration of the observation windows τ₃ in scheme B1 without         refocusing pulses (•) and 2 τ₄ (2 τ₄=τ₃ in case the duration of         the refocussing pulse is neglected) in scheme B2 using π         refocusing pulses (∘), averaging signals sampled at a rate of         500 kHz in each interval, and adapting τ₂ to keep a constant         dwell time Δt=50 ms. The lines are drawn to guide the eye.     -   b, Apparent scalar coupling constant J_(IS) ^(app) in         2,3-dibromothiophene observed as a function of the duration of         τ₃ in scheme B1 (•) or in scheme B2 (∘) with a constant dwell         time Δt=50 ms.     -   c, Signal-to-noise ratio (S/N) for the same sample of         2,3-dibromothiophene determined with scheme B2 with 100 μs<τ₃<2         ms. The black line shows a fit to the function S/N˜τ₃ ^(1/2);

FIG. 4 shows a comparison of NMR spectra in a homogeneous and an inhomogeneous magnetic field.

-   -   a, Conventional (single-quantum) NMR spectra of the same sample         of 2,3-dibromothiophene as in FIG. 2, obtained by Fourier         transformation of an FID measured at 11.7 T (500 MHz for         protons), with the magnet shimmed to yield a line-width Δν*˜1.2         Hz and deliberately de-shimmed to yield a line-width Δν*˜20 Hz.     -   b, LLC spectra observed ‘on the fly’ of a sample of         2,3-dibromothiophene in a homogeneous (<Δν_(LLC)>=17.5±0.2 mHz         and J_(IS) ^(app)=5.741 Hz±0.1 mHz) and inhomogeneous field         (<Δν_(LLC)>=22.8±0.4 mHz and J_(IS) ^(app)=5.744 Hz±0.2 mHz). In         a poorly shimmed magnetic field, some broadening (+5.3 mHz) and         a slight error in J_(IS) ^(app) (+3 mHz) are thus observed. The         areas of the peaks are identical. The LLC's were excited with         sequence A3 and sustained and observed with sequence B2 of FIG.         1 with the following parameters: τ₄4=500 μs, Δt=τ₂+τ₃=50 ms, rf         amplitude of CW sustaining field γB1/(2π)=4.5 kHz;

FIG. 5 shows ‘on the fly’ LLC's according to the invention in a weakly oriented medium. The LLC spectra of 3-bromothiophene-2-carboxylic acid in a (1:1) D₂O/DMSO-d₆ with and without addition of a very small amount (0.25%) of C₅E₁₂ were observed ‘on the fly’ at B₀=11.7 T (500 MHz for protons) and T=300 K. The isotropic solution shows J_(IS) ^(app)=5252.0±0.2 mHz and <Δν>≈18.5 mHz whereas the weakly aligned medium gives T_(IS) ^(app)=J_(IS) ^(app)+2D_(IS) ^(app)=5241.3±0.2 mHz and <Δν>≈40.0 mHz, hence 2D_(IS) ^(app)=−10.7±0.4 mHz. The LLC's were excited with sequence A3 and sustained and observed with sequence B2 of FIG. 1 with the following parameters: τ₃/2=500 μs, Δt=τ₂+τ₃=50 ms, rf amplitude of CW sustaining field γB₁/(2π)=4.5 kHz;

FIG. 6 shows hyperpolarized ‘on the fly’ LLC spectra of 3-Bromothiophene-2-carboxylic acid, showing a 300-fold enhancement of the signal intensity.

-   -   a, The sample consisted of 20 μL of a 50 mM solution of         3-bromothiophene-2-carboxylic acid in a 3:2 DMSO-d₆/D₂O (v/v)         mixture, doped with 30 mM TEMPO, rapidly frozen, immersed in a         field of 3.35 T, hyperpolarized by 30 mW microwave irradiation         at 93.89 GHz at 1.2 K during 300 s, and dissolved with 3 mL of         preheated D₂O to a final concentration of 250 vLIVI         3-bromothiophene-2-carboxylic acid. The hyperpolarized sample         was rapidly transferred to B₀=11.7 T (500 MHz for protons) at         T=296 K, and the LLC was then excited with uence A3, sustained         and observed with sequence B2 of FIG. 1 with the following         parameters: τ₃/2=100 μs, Δt=τ₂+τ₃=50 ms, rf amplitude of CW         sustaining field γB₁/(2π)=4.5 kHz, offsets         Ω₁/(2π)=−Ω_(S)/(2π)=103 Hz, the rf carrier being set half-way         between the two chemical shifts.     -   b, Thermal equilibrium signal (i.e., without DNP) of the same         sample measured with the same parameters, but with 256 scans and         multiplied by a factor 10.

DESCRIPTION OF THE PREFERRED EMBODIMENT

In an experiment according to the invention, the signals are observed during brief interruptions (observation interval τ₃) of a sustaining rf field (scheme B1 in FIG. 1). This leads to a temporary conversion of LLC's into observable magnetization, e.g. I_(x)−S_(x). In the simplest version of the inventive method, the observation intervals τ₃ are kept below 0.1 ms, so that the evolution of I_(x)−S_(x) under chemical shifts, couplings and transverse relaxation can be neglected (FIG. 1 B1). In a more sophisticated variant of the inventive method, the sensitivity can be improved by increasing the duration of the observation intervals τ₃ beyond 0.1 ms, and by inserting π refocusing pulses in the centre of the observation intervals τ₃ (one refocusing pulse in each observation interval τ₃) to refocus chemical shifts (scheme B2 in FIG. 1).

In the example shown in FIG. 1 the initial populations, described by the density operator σ=I_(z)+S_(z) (which may be enhanced by DNP), is transformed into σ=I_(x)−S_(x). Scheme A1 of FIG. 1 starts with a non-selective (π/2)_(x) pulse to excite the state σ=−I_(y)−S_(y) followed by a delay τ₁=1/(2|ΔΩ_(IS)|), where ΔΩ_(IS)=Ω_(I)−Ω_(S). Since the rf carrier frequency is normally positioned half-way between the two chemical shifts at ω_(rf)=(Ω₁+Ω_(S))/2, σ=−I_(y)−S_(y) is transformed into σ=I_(x)−S_(x) during the delay τ₁. The precession under J_(IS) in the interval τ₁ can usually be neglected in weakly coupled systems where 2πJ_(IS)<<ΔΩ_(IS).

In scheme A2, a semi-selective IC pulse applied to either spins I or S to invert the populations across either of the two doublets is immediately followed by a non-selective (π/2)_(y) pulse to excite σ=I_(x)−S_(x).⁸⁻⁹ In aqueous solutions, it may be necessary to suppress the intense HDO peak.

Scheme A3 uses an echo sequence (π/2)_(x)−τ−(π)_(x) ^((I,S))−τ− with a band-selective refocusing pulse that acts on spins I and S but is too weak to refocus the solvent resonance. The two pulsed field gradients (PFG's) G₁ lead to dephasing of all magnetization components with offsets that lie outside the range of the band-selective refocusing pulse. Like in scheme A1, σ=I_(x)−S_(x) is created after a delay, in scheme A3 the delay is 2τ+τ₁=2τ+1/(2|ΔΩ_(IS)|).

Finally, scheme A4 uses a ‘long-lived state filter’ as explained elsewhere¹⁵. The latter two schemes also have the advantage of avoiding possible radiation damping induced by large HDO signals, especially when enhanced by DNP.

Both schemes B1 and B2 in FIG. 1 rely on a continuous-wave (CW) rf field for ‘sustaining’ or ‘locking’ the LLC, to suppress the chemical shifts of spins I and S, with a carrier ω_(rf)=(Ω_(I)+Ω_(S))/2 and an rf amplitude that is usually chosen to be larger than the offset ω₁>|Ω_(I)−Ω_(S)|/2. More sophisticated methods may also be used to sustain LLC's over greater bandwidths as described elsewhere.²⁴ During rf irradiation, the eigenstates of the Hamiltonian are converted from the product base into the singlet-triplet base.⁹ In the process, the density operator τ=I_(x)—S_(x) is converted into σ=(|S₀

T₀|+|T₀

S₀|), i.e., into a zero-quantum coherence spanning the central triplet state T₀=N(|αβ

+βα

) and the singlet state S₀=N(|αβ

−|βα

) where N=2^(−1/2). In the windows τ₃ or τ₃/2, where the rf field is switched off, the density operator is briefly converted back into single-quantum coherences σ=I_(x)−S_(x), so that signals can be observed. In both schemes B1 and B2 in FIG. 1, the LLC's are sustained during the intervals τ2, while the signals are detected in the windows τ3 or τ₃/2.

The sustain-observe cycles are repeated n times, resulting in ‘sustained induction decays’ (SID's) with a total length t^(max)=nΔt digitised at intervals Δt. These Δt intervals are equivalent to the ‘dwell times’ of ordinary free induction decays. The signals can be Fourier transformed, giving a frequency domain spectrum with a digital resolution that is determined by 1/t^(max) and a spectral width 1/Δt that should be larger than the total coupling 2T=2J+4D if one wishes to avoid aliasing.

‘Windowed acquisition’ has been used previously in solid-state NMR methods such as WAHUHA, MREV and their numerous variants²⁵⁻²⁶ and for homonuclear dipolar decoupling with shaped rf pulses in the manner of DUMBO.²⁷ If the observation windows are too short, the signals can be perturbed by transient effects due to transmitter break-through, bearing in mind that the preamplifier must be protected during rf irradiation, and that this protection must be removed in the windows. On the other hand, if the observation windows are too long, the single-quantum coherences σ=I_(x)−S_(x) will decay through transverse T₂ relaxation, dephase in the inhomogeneous static field, and evolve under the chemical shifts and scalar couplings. With an analogue-to-digital converter (ADC) running at 500 kHz, one can acquire a sample point every 2 μs, and take averages over all points recorded in each observation interval τ₃ of scheme B1 or in the first and/or second τ₃/2 interval of scheme B2. Reducing the number of sampling points leads to a loss in signal-to-noise ratio. In practice, the dead time between the point where the CW rf field is switched off and where the signal can be observed is typically 3 μs, so that 8 sampling points can be taken in each window if τ₃=20 μs, or 498 points in each window if τ₃=1000 μs. If the sustaining intervals in scheme B1 of FIG. 1 are adjusted to keep a constant dwell time Δt=τ₂+τ³=50 ms so that a spectral width is 1/Δt=20 Hz or ±10 Hz, windows τ₃=20 μs or 1000 μs, lead to rf duty cycles of 99.96 or 98% respectively.

During the irradiation intervals τ₂, the coherence Q_(LLC)=(|S₀

T_(0|+|T) ₀

S₀|) evolves under the effect of the total coupling 2T_(IS)=2J_(IS)+4D_(IS) and decays with the relaxation rate R_(LLC)=R_(LLC)=1/T_(LLC)

$\begin{matrix} {{\frac{}{t}Q_{LLC}} = {{- \left( {R_{LLC} + {i\; 2\pi \; T_{IS}}} \right)} \cdot Q_{LLC}}} & (1) \end{matrix}$

In terms of the usual Cartesian product operators, this leads to:

σ₂[(I _(x) −S _(x))cos(2πT _(IS)τ2)+(2I _(y) S _(z)−2I _(z) S _(y))sin(2πT _(IS)τ₂)]·exp(−τ₂ ·R _(LLC))  (2)

This is consistent with recent work⁹, but our initial papers underestimated the effect of the couplings by a factor 2. During each observation window τ₃ in the scheme B1 of FIG. 1, the density operator evolves under the chemical shifts and again under the total coupling constant T is, albeit reduced by a factor 2, and decays with the single-quantum relaxation rate R₂=1/T₂. The overall effect for each sustain-and-observe cycle Δt=τ₂+τ₃ in scheme B1 can be written:

τ₃=cos(ΔΩ_(IS)/2·τ₃)[(I _(x) −S _(x))cos(2πT _(IS) Δt′)+(2I _(y) S _(z)−2I _(z) S _(y))sin(2πT ^(IS) Δt′)]·exp(−<R>Δt)+sin(ΔΩ_(IS)/2·τ₃)[(I _(x) S _(x))cos(2πT _(IS) Δt′)+(2I _(y) S _(z)+2I _(z) S _(y))sin(2πT _(IS) Δt′)]·exp(−<R>Δt)  (3)

Where Δt′=τ₂+τ₃/2=Δt−τ₃/2, reflecting the scaling of the total coupling constant when the rf field is switched off. We can define and apparent total coupling constant:

T _(IS) ^(app) =T _(IS) Δt′/Δt  (4)

Using the notation R₂=R_(SQC)=κR_(LLC) with κ≦9, the average decay rate <R> in Eq. (3) is

$\begin{matrix} {{< R>={\frac{1}{\Delta \; t}\left( {{\tau_{2}R_{LLC}} + {\tau_{3}R_{2}}} \right)}} = {\frac{\tau_{2} + \tau_{3}}{\tau_{2} + \tau_{3}}R_{LLC}}} & (5) \end{matrix}$

For κ=3, τ₂=49.98 ms and τ₃=20 μs, this amounts to a mere 0.08% increase in the average relaxation rate and hence to a negligible contribution to the line-width. When the CW rf field along the x-axis is switched on again, the differences I_(x)−S_(x) and 2I_(y)S_(z)−2I_(z)S_(y) resume their identity as LLC's, while the sum I_(x)+S_(x) is spin-locked and decays, and the sum 2I_(y)S_(z)+2I_(z)S_(y) is dephased under the effect of the rf field inhomogeneity. With a chemical shift difference ΔΩ_(IS)/(2π)=300 Hz, we have cos(ΔΩ_(IS) τ₃)=0.9993˜1. This infinitesimal ‘leakage’ of the LLC may seem negligible, but it is amplified as the sustain-observe sequence is repeated n times with cos(ΔΩ_(IS) τ₃)^(n) so that cos(ΔΩ_(IS) τ₃)¹⁰⁰=0.936, thus affecting the decay of the LLC. The resulting time domain signals sampled at intervals Δt are

$\begin{matrix} {{{I\left( {n\; \Delta \; t} \right)} = {I_{0}{{\cos \left( {2\; \pi \; T_{IS}n\; \Delta \; t^{\prime}} \right)} \cdot {\exp \left\lbrack {{- n}\; \Delta \; {t \cdot \left( {{\frac{\tau_{2}}{\tau_{2} + \tau_{3}} \cdot R_{LLC}} + {\frac{\tau_{3}}{\tau_{2} + \tau_{3}} \cdot R_{2}}} \right)}} \right\rbrack}}{\cos \left( {\Delta \; \Omega_{IS}\tau_{3}} \right)}^{n}}}\mspace{20mu} {\ldots = {I_{0}{{\cos \left( {2\; \pi \; T_{IS}^{app}n\; \Delta \; t} \right)} \cdot {\exp \left( {{{- n}\; \Delta \; {t \cdot}} < R >} \right)}}{\cos \left( {\Delta \; \Omega_{IS}\tau_{3}} \right)}^{n}}}} & (6) \end{matrix}$

In order to suppress contributions from I_(x)+S_(x) and 2I_(y)S_(z)+2I_(z)S_(y), scheme B2 uses a π pulse in the middle of each observation window to refocus the chemical shifts. As a result, the density operator at the end of each window τ₃ in scheme B2 is:

σ₇=[(I _(x) −S _(x))cos(2πT _(IS) Δt′)+(2I _(y) S _(z)−2I _(z) S _(y))sin(2πT _(IS) Δt′)]·exp(−<R>Δt)  (7)

The resulting time domain signals sampled at intervals Δt are:

$\begin{matrix} {{{{I\left( {n\; \Delta \; t} \right)} = {I_{0}{{\cos \left( {2\; \pi \; T_{IS}n\; \Delta \; t^{\prime}} \right)} \cdot {\exp \left\lbrack {{- n}\; \Delta \; {t \cdot \left( {{\frac{\tau_{2}}{\tau_{2} + {2\tau_{4}}} \cdot R_{LLC}} + {\frac{\tau_{3}}{\tau_{2} + \tau_{3}} \cdot R_{2}}} \right)}} \right\rbrack}}}}\; \mspace{20mu} {\ldots = {I_{0}{{\cos \left( {2\; \pi \; T_{IS}^{app}n\; \Delta \; t} \right)} \cdot {\exp \left( {{{- n}\; \Delta \; {t \cdot}} < R >} \right)}}}}}\mspace{59mu}} & (8) \end{matrix}$

Experimental Evidence

FIG. 2 e shows a ‘sustained induction decay’ (SID) that can be compared with the FID presented in FIG. 2 a and with the modulated echo decay of FIG. 2 c. The three signals stem from the two protons in an isotropic solution (where T_(IS)=J_(IS)) of 2,3-dibromothiophene (20 mM in DMSO-d₆ with 30 mM ascorbic acid²⁸ to scavenge paramagnetic oxygen), recorded with a simple π/2 pulse (FIG. 2 a), observed in a J-resolved 2D manner²⁹ (FIG. 2 c), and recorded ‘on the fly’ LLC's in windows τ₃/2=100 is according to the invention with scheme B2 (FIG. 2 e). Their Fourier transforms are presented in FIGS. 2 b, 2 d and 2 f respectively. The LLC's ‘SID’ signal is described by Eq. (8) and slowly decays with a time-constant <T>=1/<R>=19.9 s. Its Fourier transforms (FIGS. 2 f and 2 g) show two lines at v=±J_(IS) separated by 2J_(IS) with line-widths <Δν>=1/(π<T>)=16.4 mHz (resolution enhanced by a factor ε_(Δ)=v/<Δν>˜180 and 8.5 with respect to conventional FID and echo modulation respectively). The fact that the couplings are twice as effective in the rotating frame than in the laboratory frame is reminiscent of total correlation spectroscopy ('TOCSY')³⁰. Note that the antiphase terms 2I_(y)S_(z)−2I_(z)S_(y) cannot induce any signals in the orthogonal channel, so that we have a case of pure amplitude (rather than phase) modulation. The ‘on the fly’ LLC spectrum according to the invention of the two diastereotopic protons of glycine in L-Ala-Gly is shown in FIG. 2 h.

FIG. 3 a shows how the insertion of refocusing pulses in the middle of the observation windows allows one to eliminate the effects of chemical shifts. For longer windows 100 is <τ₃<2 ms, scheme B2 provides longer decays and hence narrower line-widths. Note that the narrowest lines are obtained, albeit at the expense of sensitivity, with scheme B1 with very short observation windows (typically τ₃=20 μs). FIG. 3 b shows how refocusing pulse allow one to obtain an accurate measurement of scalar couplings J_(IS) (or total couplings T_(IS) in anisotropic media) even for long observation windows τ₃. (The slight decrease in J_(IS) ^(app) for long τ₃ is described by Eq. (4)). Finally, FIG. 3 c shows how longer observation windows τ₃, which allow one to average over a larger number of data points in each window, result in improved signal-to-noise ratios, which are proportional to τ₃ ^(1/2).

In principle, the evolution of LLC's is immune to the inhomogeneity of the magnetic field if one uses the scheme B2 of FIG. 1. We should remember however that all excitation schemes A1-A4 of FIG. 1 require one to distinguish the chemical shifts of the two spins I and S, although it is not necessary to resolve their mutual coupling constant. The methods can thus tolerate a moderate inhomogeneity of the static field, as long as the line-widths fulfil the condition Δν*=1/(πT₂)*<ΔΩ_(IS).

FIG. 4 shows how a deliberate missetting of the shim currents (z₁, z₂, z₃, x, y, z₀x, and z₀y) to broaden the line-widths in the conventional (single-quantum) spectrum to about Δν*=20 Hz has little effect on the averaged line-widths <Δν> of the LLC's and the apparent scalar couplings J_(IS) ^(app) (+5.3 and +3 mHz, respectively). Ex-situ NMR⁴⁻⁵ and MRI in moderately inhomogeneous fields (e.g., in the vicinity of discontinuities of the magnetic susceptibility) may benefit from this property.

Very weak molecular alignments, yielding minute residual dipolar couplings (RDC's) in the mHz range, can be readily determined with the inventive method. FIG. 5 shows the ‘on the fly’ LLC spectra according to the invention of two solutions of 3-bromothiophene-2-carboxylic acid in (1:1) D₂O/DMSO-d₆, with and without addition of a 0.25% pentaethylene glycol monododecyl ether (C₁₂E₅). The very weak alignement of the solute gives rise to a net RDC with 2-D_(IS) ^(app)=−10.7±0.4 mHz. The order parameter of the r_(HH) vector that connects the two protons in 3-bromothiophene-2-carboxylic acid can be estimated to be as small as S≦(2.52±0.10)·10⁻⁶ (assuming that the internuclear distance is r_(HH)=2.662 Å like in thiophene³¹, and assuming that the average r_(HH) vector is oriented along B₀, i.e., θ=0).

Since LLC spectra can be recorded in a single scan, they can be boosted by ‘dissolution’ DNP. Spectra of a 20 μL solution of 50 mM 2,3-dibromothiophene dissolved in a 3:2 DMSO-d₆/D₂O (v/v) mixture doped with 30 mM TEMPOL are compared in FIG. 6 with and without hyperpolarization by ‘dissolution’ DNP (see Methods section below). The dissolution, transfer and injection required 3.2 s. After an additional 3 s of settling time in the NMR tube, some bubbles and convection currents cannot be ruled out. These tend to broaden ordinary (single-quantum) line-widths, but have little effect on LLC spectra. The LLC's were excited, sustained, and observed with sequences A3 and B2 of FIG. 1. The enhancement was ε_(DNP)≈300. It may be possible to improve this performance by preventing losses of the proton polarization due to relaxation in low fields during the voyage between the DNP polariser and the NMR magnet.³²

Methods Sample Preparation DNP Sample:

a 20 μL solution of 50 mM 3-bromothiophene-2-carboxylic acid (97%, Aldrich) dissolved in a 3:2 mixture of DMSO-d₆/D₂O (v/v) (99.98%, Aldrich) doped with 30 mM 4-Hydroxy-2,2,6,6-tetramethylpiperidine 1-oxyl (TEMPOL) (purum, ≧97.0%, Fluka). The freshly prepared mixture was rapidly frozen in liquid nitrogen to form 104 beads.

Ascorbate Scavenger:

a 3 M D₂O solution of sodium L-ascorbate (≧99%, Aldrich) was prepared and rapidly frozen in liquid nitrogen (104 beads).

NMR Samples:

a 20 mM isotropic solution of 2,3-dibromothiophene (98% Aldrich) in DMSO-d₆ with addition of 30 mM L-ascorbic acid (BioXtra, ≧99.0%, Sigma) for scavenging paramagnetic oxygen was prepared and sealed in a 5 mm NMR tube.

Aligned Media:

Two 50 mM solution of 3-bromothiophene-2-carboxylic acid in a (1:1) D₂O/DMSO-d₆ mixture with addition of 30 mM L-ascorbic acid for scavenging paramagnetic oxygen were prepared, one with and the other without addition of 0.25% of pentaethylene glycol monododecyl ether (C₁₂E₅, Sigma ≧98%) for partial alignment, and sealed in 5 mm NMR tubes.

Peptide Sample:

A 0.5 M solution of L-ala-gly (Sigma) in D₂O with addition of 30 mM sodium L-ascorbate (≧99%, Aldrich) was prepared and sealed in a 5 mm NMR tube. All chemicals were used without further purification.

Hyperpolarization

DNP was performed by thermal mixing at 1.2 K and 3.35 T in a home-built ‘dissolution’ DNP polarizer³³⁻³⁵ by applying a CW microwave irradiation at f_(μw)=93.89 GHz and P_(μw)=30 mW for 5 minutes. The DNP build-up of ¹H magnetization is fast (τ_(DNP)˜120 s) and yields high proton spin polarization P(¹H)˜20-40% depending on sample composition.³⁶ About 20 μL of frozen beads of the polarized sample, together with 90 μL of frozen beads of a 3 M D₂O solution of sodium ascorbate, were rapidly dissolved with 3 mL of preheated D₂O (T=440 K and P=1.2 MPa) and intimately mixed within 700 ms, transferred in 1.5 s to a 11.7 T NMR magnet through a 1 mm inner diameter PTFE tube pressurized with helium gas at 0.6 MPa, and allowed to settle for 0.5 s, prior to injection into a pre-locked NMR tube, which required another 0.5 s. After a further 3 s settling time in the NMR tube to allow turbulences to slow down, the LLC was excited, sustained, and observed with the sequences A3 and B2 of FIG. 1.

NMR Measurements

NMR measurements were performed on a 500 MHz spectrometer equipped with an Inverse 5 mm Bruker CryoProbe™. The ‘on the fly’ LLC pulse program and excitation/acquisition sequences were designed and performed with TopSpin 2.1.

In conclusion, the present invention describes an ‘on-the-fly’ method where the radio-frequency (rf) irradiation required to sustain the LLC's in high magnetic field is briefly interrupted, normally at regular intervals, so that the LLC's are temporarily converted into single-quantum coherences (SQC's) that can be observed. The method according to the invention allows one to obtain ultra high-resolution spectra of long-lived coherences (LLC's) ‘on the fly’ in one-dimensional fashion by time-shared ‘windowed acquisition’. This allows one to determine very accurate total couplings T=J+2D. The method can be applied to either isotropic or anisotropic phases, providing ultra-high resolution even in moderately inhomogeneous magnetic fields. The signals can be enhanced by “dissolution” DNP¹⁰. The technique has been applied to pairs of spins in this study, but it is intended to extend the scope of application of ‘on the fly’ LLC's in the near future to multiple spin systems (N>2) with broad-band excitation and detection (replacing CW by composite pulses) of several LLC's in the same molecule or in mixtures. Since inhomogeneous fields are not detrimental to LLC's, ex-situ or in-cell studies should be readily feasible with unprecedented linewidths, and since the long lifetimes of LLC's are exquisitely sensitive to the presence of paramagnetic species²⁸, we believe they should be sensitive probes for the detection paramagnetic species such as oxygen.

REFERENCES

-   1. Ernst, R. R. & Anderson, W. A. Application of Fourier transform     spectroscopy to magnetic resonance. Rev. Sci. Instrum. 37, 93     (1966). -   2. Allerhand, A., Addleman, R. E. & Osman, D. Ultrahigh resolution     NMR. 1. General considerations and preliminary results for C-13     NMR. J. Am. Chem. Soc. 107, 5809-5810 (1985). -   3. Balbach, J. J., Conradi, M. S., Cistola, D. P., Tang, C. G.,     Garbow, J. R. & Hutton, W. C. High-resolution NMR in inhomogeneous     fields. Chem. Phys. Lett. 277, 367-374 (1997). -   4. Appelt, S., Kuhn, H., Hasing, F. W. & Blumich, B. Chemical     analysis by ultrahigh-resolution nuclear magnetic resonance in the     earth's magnetic field. Nat. Phys. 2, 105-109 (2006). -   5. Meriles, C. A., Sakellariou, D., Heise, H., Moule, A. J. &     Pines, A. Approach to high-resolution ex situ NMR spectroscopy.     Science 293, 82-85 (2001). -   6. Pelupessy, P., Rennella, E. & Bodenhausen, G. High-resolution NMR     in magnetic fields with unknown spatiotemporal variations. Science     324, 1693-1697 (2009). -   7. Pileio, G., Carravetta, M. & Levitt, M. H. Extremely     Low-Frequency Spectroscopy in Low-Field Nuclear Magnetic Resonance.     Phys. Rev. Lett. 103, 083002 (2009). -   8. Sarkar, R., Ahuja, P., Vasos, P. R. & Bodenhausen, G. Long-lived     coherences for homogeneous line narrowing in spectroscopy. Phys.     Rev. Lett. 104, 053001 (2010). -   9. Sarkar, R., Ahujab, P., Vasos, P. R., Bornet, A., Wagnieres, O. &     Bodenhausen, G. Long-lived coherences for line-narrowing in     high-field NMR. Prog. Nucl. Magn. Reson. -   Spectrosc., in press (2011). -   10. Ardenkjaer-Larsen, J. H., Fridlund, B., Gram, A., Hansson, G.,     Hansson, L., Lerche, M. H., Servin, R., Thaning, M. & Golman, K.     Increase in signal-to-noise ratio of >10,000 times in liquid-state     NMR. Proc. Natl. Acad. Sci. U.S.A. 100, 10158-10163 (2003). -   11. Freeman, R. & Hill, H. D. W. Dynamic nuclear magnetic resonance     spectroscopy, (Academic Press, New York, 1975). -   12. Bodenhausen, G., Freeman, R. & Turner, D. L. Two-dimensional J     spectroscopy: proton-coupled carbon-13 NMR. J. Chem. Phys. 65,     839-840 (1976). -   13. Bodenhausen, G., Freeman, R., Morris, G. A. & Turner, D. L.     Proton-coupled carbon-13 J spectra in the presence of strong     coupling. II. J. Magn. Reson. 28, 17-28 (1977). -   14. Pelupessy, P., Duma, L. & Bodenhausen, G. Improving resolution     in single-scan 2D spectroscopy. J. Magn. Reson. 194, 169-174 (2008). -   15. Bornet, A., Sarkar, R. & Bodenhausen, G. Life-times of     long-lived coherences under different motional regimes. J. Magn.     Reson. 206, 154-156 (2010). -   16. Carravetta, M., Johannessen, O. G. & Levitt, M. H. Beyond the     T-1 limit: Singlet nuclear spin states in low magnetic fields. Phys.     Rev. Lett. 92, 153003-153007 (2004). -   17. Carravetta, M. & Levitt, M. H. Theory of long-lived nuclear spin     states in solution nuclear magnetic resonance. I. Singlet states in     low magnetic field. J. Chem. Phys. 122, 214505 (2005). -   18. Sarkar, R., Vasos, P. R. & Bodenhausen, G. Singlet-state     exchange NMR spectroscopy for the study of very slow dynamic     processes. J. Am. Chem. Soc. 129, 328-334 (2007). -   19. Pileio, G. & Levitt, M. H. Theory of long-lived nuclear spin     states in solution nuclear magnetic resonance. II. Singlet spin     locking. J. Chem. Phys. 130, 214501 (2009). -   20. Ahuja, P., Sarkar, R., Vasos, P. R. & Bodenhausen, G. Long-lived     States in Multiple-Spin Systems. Chem. Phys. Chem. 10, 2217-2220     (2009). -   21. Vasos, P. R., Comment, A., Sarkar, R., Ahuja, P., Jannin, S.,     Ansermet, J. P., Konter, J. A., Hautle, P., van den Brandt, B. &     Bodenhausen, G. Long-lived states to sustain hyperpolarized     magnetization. Proc. Natl. Acad. Sci. U.S.A. 106, 18475-18479     (2009). -   22. Frydman, L. & Blazina, D. Ultrafast two-dimensional nuclear     magnetic resonance spectroscopy of hyperpolarized solutions. Nat.     Phys. 3, 415-419 (2007). -   23. Pelupessy, P. Adiabatic single scan two-dimensional NMR     spectrocopy. J. Am. Chem. Soc. 125, 12345-12350 (2003). -   24. Sarkar, R., Ahuia, P., Moskau, D., Vasos, P. R. &     Bodenhausen, G. Extending the scope of singlet-state spectroscopy.     Chem. Phys. Chem. 8, 2652-2656 (2007). -   25. Waugh, J. S., Huber, L. M. & Haeberlen, U. Approach to     high-resolution NMR in solids. Phys. Rev. Lett. 20, 180 (1968). -   26. Rhim, W. K., Elleman, D. D. & Vaughan, R. W. Enhanced resolution     for solid state NMR. J. Chem. Phys. 58, 1772-1773 (1973). -   27. Lesage, A., Sakellariou, D., Hediger, S., Elena, B., Charmont,     P., Steuernagel, S. & Emsley, L. Experimental aspects of proton NMR     spectroscopy in solids using phase-modulated homonuclear dipolar     decoupling. J. Magn. Reson. 163, 105-113 (2003). -   28. Miéville, P., Ahuja, P., Sarkar, R., Jannin, S., Vasos, P. R.,     Gerber-Lemaire, S., Mishkovsky, M., Comment, A., Gruetter, R.,     Ouari, O., Tordo, P. & Bodenhausen, G. Scavenging free radicals to     preserve enhancement and extend relaxation times in NMR using     dynamic nuclear polarization. Angew. Chem. Intern. Ed. 49, 6182-6185     (2010). -   29. Aue, W. P., Karhan, J. & Ernst, R. R. Homonuclear broad-band     decoupling and 2-dimensional J-resolved NMR-spectroscopy. J. Chem.     Phys. 64, 4226-4227 (1976). -   30. Braunschweiler, L. & Ernst, R. R. Coherence transfer by     isotropic mixing—application to proton correlation spectroscopy. J.     Magn. Reson. 53, 521-528 (1983). -   31. Bak, B., Christensen, D., Hansen-Nygaard, L. &     Rastrup-Andersen, J. The structure of thiophene. J. Mol. Spectrosc.     7, 58-63 (1961). -   32. MiCville, P., Jannin, S. & Bodenhausen, G. Relaxometry of     insensitive nuclei: optimizing dissolution dynamic nuclear     polarization. J. Magn. Reson., in press (2011). -   33. Comment, A., van den Brandt, B., Uffmann, K., Kurdzesau, F.,     Jannin, S., Konter, J. A., Hautle, P., Wenckebach, W. T. H.,     Gruetter, R. & van der Klink, J. J. Design and performance of a DNP     prepolarizer coupled to a rodent MRI scanner. Concepts Magn. Reson.     B 31B, 255-269 (2007). -   34. Comment, A., van den Brandt, B., Uffmann, K., Kurdzesau, F.,     Jannin, S., Konter, J. A., Hautle, P., Wenckebach, W. T.,     Gruetter, R. & van der Klink, J. J. Principles of operation of a DNP     prepolarizer coupled to a rodent MRI scanner. Appl. Magn. Reson. 34,     313-319 (2008). -   35. Jannin, S., Comment, A., Kurdzesau, F., Konter, J. A., Hautle,     P., van den Brandt, B. & van der Klink, J. J. A 140 GHz prepolarizer     for dissolution dynamic nuclear polarization. J. Chem. Phys. 128,     241102 (2008). -   36. Kurdzesau, F., van den Brandt, B., Comment, A., Hautle, P.,     Jannin, S., van der Klink, J. J. & Konter, J. A. Dynamic nuclear     polarization of small labelled molecules in frozen water-alcohol     solutions. J. Phys. D: Appl. Phys. 41, 155506 (2008). 

1. A method for nuclear magnetic resonance (NMR) spectroscopy of a sample, the method comprising the steps of: a) exciting long lived coherences (LLC) between a singlet state S₀ and a central triplet state T₀ of nuclei of the sample by irradiating the sample with an rf-field having a carrier frequency ω_(rf); b) sustaining the LLC by maintaining rf-irradiation during an interval τ₂; c) temporarily converting the LLC into observable magnetisation by interrupting the rf-irradiation during an observation interval τ₃; d) detecting NMR-signals during the observation interval τ₃; e) reconverting the observable magnetisation back into LLC after the observation interval τ₃; and f) repeating steps (b) to (e) n times, wherein n is a positive integer.
 2. The method of claim 1, wherein the LLC are excited by transforming an initial spin polarization, (I_(z)+S_(z)) into single quantum coherences (I_(x)−S_(x)) or (I_(y)−S_(y)) or (2I_(y)S_(z)−2I_(z)S_(y)) or (2I_(x)S_(z)−2I_(z)S_(x)) prior to initiating irradiation of the sample with the rf-field.
 3. The method of claim 2, wherein the initial spin polarization is a thermal equilibrium Boltzmann distribution.
 4. The method of claim 1, wherein the sample is hyperpolarized, thereby enhancing a spin polarization (I_(z)+S_(z)) and thus enhancing LLC that are subsequently excited by transforming the enhanced spin polarization (I_(z)+S_(z)) into enhanced single quantum coherences ((I_(x)−S_(x)) or (I_(y)−S_(y)) or (2I_(y)S_(z)−2I_(z)S_(y)) or (2I_(x)S_(z)−2I_(z)S_(x)) prior to initiating irradiation of the sample with the rf-field.
 5. The method of claim 4, wherein the sample is hyperpolarized using dynamic nuclear polarization.
 6. The method of claim 1, wherein the carrier frequency is ω_(rf)=(Ω_(I)−Ω_(S))/2, with Ω_(I): chemical shift of nuclei of the sample with spin I, Ω_(S): chemical shift of nuclei of the sample with spin S.
 7. The method of claim 1, wherein the rf-field is a continuous-wave rf-field.
 8. The method of claim 1, wherein the rf-field is modulated in amplitude.
 9. The method of claim 1, wherein the rf-field is modulated in phase.
 10. The method of claim 6, wherein an amplitude of the rf-field is larger than an offset |Ω_(I)−Ω_(S)|/2.
 11. The method of claim 1, wherein a refocusing pulse is applied in a middle of the observation interval τ₃.
 12. The method of claim 1, wherein an NMR spectroscopy measurement is carried out in a single experiment. 